دورية أكاديمية
Lack of association for reported endocrine pancreatic cancer risk Loci in the PANDoRA consortium
| العنوان: | Lack of association for reported endocrine pancreatic cancer risk Loci in the PANDoRA consortium |
|---|---|
| المؤلفون: | Campa D., Obazee O., Pastore M., Panzuto F., Lico V., Greenhalf W., Katzke V., Tavano F., Costello E., Corbo V., Talar-Wojnarowska R., Strobel O., Zambon C. F., Neoptolemos J. P., Zerboni G., Kaaks R., Key T. J., Lombardo C., Jamroziak K., Gioffreda D., Hackert T., Khaw K. -T., Landi S., Milanetto A. C., Landoni L., Lawlor R. T., Bambi F., Pirozzi F., Basso D., Pasquali C., Capurso G., Canzian F. |
| المساهمون: | Campa, D., Obazee, O., Pastore, M., Panzuto, F., Lico, V., Greenhalf, W., Katzke, V., Tavano, F., Costello, E., Corbo, V., Talar-Wojnarowska, R., Strobel, O., Zambon, C. F., Neoptolemos, J. P., Zerboni, G., Kaaks, R., Key, T. J., Lombardo, C., Jamroziak, K., Gioffreda, D., Hackert, T., Khaw, K. -T., Landi, S., Milanetto, A. C., Landoni, L., Lawlor, R. T., Bambi, F., Pirozzi, F., Basso, D., Pasquali, C., Capurso, G., Canzian, F. |
| بيانات النشر: | American Association for Cancer Research Inc. |
| سنة النشر: | 2017 |
| المجموعة: | Sapienza Università di Roma: CINECA IRIS |
| مصطلحات موضوعية: | pancreatic endocrine tumor, polymorphism |
| الوصف: | Background: Pancreatic neuroendocrine tumors (PNETs) are rare neoplasms for which very little is known about either environmental or genetic risk factors. Only a handful of association studies have been performed so far, suggesting a small number of risk loci. Methods: To replicate the best findings, we have selected 16 SNPs suggested in previous studies to be relevant in PNET etiogenesis. We genotyped the selected SNPs (rs16944, rs1052536, rs1059293, rs1136410, rs1143634, rs2069762, rs2236302, rs2387632, rs3212961, rs3734299, rs3803258, rs4962081, rs7234941, rs7243091, rs12957119, and rs1800629) in 344 PNET sporadic cases and 2, 721 controls in the context of the PANcreatic Disease ReseArch (PANDoRA) consortium. Results: After correction for multiple testing, we did not observe any statistically significant association between the SNPs and PNET risk. We also used three online bioinformatic tools (HaploReg, RegulomeDB, and GTEx) to predict a possible functional role of the SNPs, but we did not observe any clear indication. Conclusions: None of the selected SNPs were convincingly associated with PNET risk in the PANDoRA consortium. Impact:Wecan exclude a major role of the selected polymorphisms in PNET etiology, and this highlights the need for replication of epidemiologic findings in independent populations, especially in rare diseases such as PNETs. Cancer Epidemiol Biomarkers Prev; 26(8); 1349-51. |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| العلاقة: | info:eu-repo/semantics/altIdentifier/pmid/28765340; info:eu-repo/semantics/altIdentifier/wos/WOS:000412226500023; volume:26; issue:8; firstpage:1349; lastpage:1351; numberofpages:3; journal:CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION; http://hdl.handle.net/11573/1623140Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85026845386 |
| DOI: | 10.1158/1055-9965.EPI-17-0075 |
| الإتاحة: | https://doi.org/10.1158/1055-9965.EPI-17-0075Test http://hdl.handle.net/11573/1623140Test |
| حقوق: | info:eu-repo/semantics/openAccess |
| رقم الانضمام: | edsbas.190E7380 |
| قاعدة البيانات: | BASE |
| DOI: | 10.1158/1055-9965.EPI-17-0075 |
|---|